1-(tert-Butoxycarbonyl)-2-methylpiperidine-2-carboxylic acid

97%

Reagent Code: #114500
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CAS Number 746658-74-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 243.30 g/mol
Formula C₁₂H₂₁NO₄
badge Registry Numbers
MDL Number MFCD09910215
thermostat Physical Properties
Boiling Point 354.3°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description Product Description

This compound is primarily used as an intermediate in organic synthesis, particularly in the pharmaceutical industry. It plays a key role in the development of active pharmaceutical ingredients (APIs) and other biologically active molecules. The tert-butoxycarbonyl (Boc) protecting group in its structure is crucial for safeguarding amine functionalities during multi-step synthetic processes, ensuring selective reactions. Its piperidine moiety is often incorporated into compounds targeting neurological and cardiovascular disorders, making it valuable for drug discovery and medicinal chemistry research. Additionally, its carboxylic acid group provides a versatile handle for further chemical modifications, enabling the creation of diverse derivatives for various applications.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days €79.82
inventory 5g
10-20 days €279.72
inventory 10g
10-20 days €489.58
1-(tert-Butoxycarbonyl)-2-methylpiperidine-2-carboxylic acid
This compound is primarily used as an intermediate in organic synthesis, particularly in the pharmaceutical industry. It plays a key role in the development of active pharmaceutical ingredients (APIs) and other biologically active molecules. The tert-butoxycarbonyl (Boc) protecting group in its structure is crucial for safeguarding amine functionalities during multi-step synthetic processes, ensuring selective reactions. Its piperidine moiety is often incorporated into compounds targeting neurological and cardiovascular disorders, making it valuable for drug discovery and medicinal chemistry research. Additionally, its carboxylic acid group provides a versatile handle for further chemical modifications, enabling the creation of diverse derivatives for various applications.
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